Methocarbamol
- Product NDC
- 76420-893
- 11-digit product format
- 764200893
- Labeler code
- 76420
- Product ID
- 76420-893_2cbe9e1b-d4dc-de70-e063-6394a90a18b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 125OD7737X | METHOCARBAMOL | 532-03-6 | METHOCARBAMOL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 76420-893-01 | 76420089301 | 100 TABLET, COATED in 1 BOTTLE (76420-893-01) | 2025-01-28 | No | No | Historical |
| 76420-893-05 | 76420089305 | 500 TABLET, COATED in 1 BOTTLE (76420-893-05) | 2025-01-28 | No | No | Historical |
| 76420-893-12 | 76420089312 | 120 TABLET, COATED in 1 BOTTLE (76420-893-12) | 2025-01-28 | No | No | Historical |
| 76420-893-30 | 76420089330 | 30 TABLET, COATED in 1 BOTTLE (76420-893-30) | 2025-01-28 | No | No | Historical |
| 76420-893-60 | 76420089360 | 60 TABLET, COATED in 1 BOTTLE (76420-893-60) | 2025-01-28 | No | No | Historical |
| 76420-893-90 | 76420089390 | 90 TABLET, COATED in 1 BOTTLE (76420-893-90) | 2025-01-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Methocarbamol Tablets Rx Only | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2025-01-28 | HUMAN PRESCRIPTION DRUG LABEL | 1 |